Does AMMONIUM\CHLORPHENIRAMINE\SODIUM Cause Condition aggravated? 30 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Condition aggravated have been filed in association with AMMONIUM\CHLORPHENIRAMINE\SODIUM. This represents 90.9% of all adverse event reports for AMMONIUM\CHLORPHENIRAMINE\SODIUM.
30
Reports of Condition aggravated with AMMONIUM\CHLORPHENIRAMINE\SODIUM
90.9%
of all AMMONIUM\CHLORPHENIRAMINE\SODIUM reports
30
Deaths
22
Hospitalizations
How Dangerous Is Condition aggravated From AMMONIUM\CHLORPHENIRAMINE\SODIUM?
Of the 30 reports, 30 (100.0%) resulted in death, 22 (73.3%) required hospitalization, and 17 (56.7%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AMMONIUM\CHLORPHENIRAMINE\SODIUM. However, 30 reports have been filed with the FAERS database.
What Other Side Effects Does AMMONIUM\CHLORPHENIRAMINE\SODIUM Cause?
Hyponatraemia (33)
Appendicitis (32)
Appendicolith (32)
Ascites (32)
Blood phosphorus increased (32)
Cardiogenic shock (32)
Multiple organ dysfunction syndrome (32)
Sepsis (32)
Ventricular fibrillation (32)
Abdominal distension (31)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)